# FDA recall D-1464-2022

> **Midlab Incorporated** · Class II · drug recall initiated 2022-08-08.

## Product

Corsair Personal Care 99X Instant Foam Hand Sanitizer (benzalkonium chloride 0.1%)128 Fl. Oz. (1 Gal.) 3.78 liters bottles, Southern Products & Services, Inc. 2515 Jake Drive Ste B, Cumming, GA 30028

## Reason for recall

CGMP Deviations: Product manufactured using expired active ingredient, Benzalkonium chloride.

## Distribution

Naionwide within the United States

## Key facts

- **Recall number:** D-1464-2022
- **Recalling firm:** Midlab Incorporated
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2022-08-08
- **Report date:** 2022-08-31
- **Termination date:** 2023-08-15

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Athens, TN, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-1464-2022

## Citation

> AI Analytics. FDA recall D-1464-2022. Retrieved 2026-07-20 from https://api.ai-analytics.org/recall/D-1464-2022. Source: US FDA. Licensed CC0.

---

*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*